Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:98446233-98446364 | Common:1; Rare:21 | ||||
chr10:98446874-98447030 | Rare:45 | ||||
chr10:99430616-99430981 | Common:3; Rare:89 | ||||
chr10:99659247-99659565 | Common:1; Rare:80 | ||||
chr10:99732070-99732351 | Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185914-100186194 | Rare:110 | ||||
chr10:100229547-100229640 | Rare:29 | ||||
chr10:100286610-100286725 | Common:4; Rare:69 | ||||
chr10:100347058-100347534 | Common:4; Rare:123 | ||||
chr10:100912669-100913086 | Common:1; Rare:123 | ||||
chr10:100913335-100913471 | Rare:33 | ||||
chr10:100969196-100969554 | Common:4; Rare:94 | ||||
chr10:100987090-100987598 | Common:1; Rare:184; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996969-100997172 | Common:2; Rare:56 | ||||
chr10:100999687-100999949 | Common:1; Rare:74 |